Back to Search Start Over

The metabolite ?-ketoglutarate extends lifespan by inhibiting ATP synthase and TOR.

Authors :
Chin, Randall M.
Fu, Xudong
Pai, Melody Y.
Vergnes, Laurent
Hwang, Heejun
Deng, Gang
Diep, Simon
Lomenick, Brett
Meli, Vijaykumar S.
Monsalve, Gabriela C.
Hu, Eileen
Whelan, Stephen A.
Wang, Jennifer X.
Jung, Gwanghyun
Solis, Gregory M.
Fazlollahi, Farbod
Kaweeteerawat, Chitrada
Quach, Austin
Nili, Mahta
Krall, Abby S.
Source :
Nature. 6/19/2014, Vol. 510 Issue 7505, p397-401. 5p.
Publication Year :
2014

Abstract

Metabolism and ageing are intimately linked. Compared with ad libitum feeding, dietary restriction consistently extends lifespan and delays age-related diseases in evolutionarily diverse organisms. Similar conditions of nutrient limitation and genetic or pharmacological perturbations of nutrient or energy metabolism also have longevity benefits. Recently, several metabolites have been identified that modulate ageing; however, the molecular mechanisms underlying this are largely undefined. Here we show that ?-ketoglutarate (?-KG), a tricarboxylic acid cycle intermediate, extends the lifespan of adult Caenorhabditis elegans. ATP synthase subunit ? is identified as a novel binding protein of ?-KG using a small-molecule target identification strategy termed drug affinity responsive target stability (DARTS). The ATP synthase, also known as complex V of the mitochondrial electron transport chain, is the main cellular energy-generating machinery and is highly conserved throughout evolution. Although complete loss of mitochondrial function is detrimental, partial suppression of the electron transport chain has been shown to extend C. elegans lifespan. We show that ?-KG inhibits ATP synthase and, similar to ATP synthase knockdown, inhibition by ?-KG leads to reduced ATP content, decreased oxygen consumption, and increased autophagy in both C. elegans and mammalian cells. We provide evidence that the lifespan increase by ?-KG requires ATP synthase subunit ? and is dependent on target of rapamycin (TOR) downstream. Endogenous ?-KG levels are increased on starvation and ?-KG does not extend the lifespan of dietary-restricted animals, indicating that ?-KG is a key metabolite that mediates longevity by dietary restriction. Our analyses uncover new molecular links between a common metabolite, a universal cellular energy generator and dietary restriction in the regulation of organismal lifespan, thus suggesting new strategies for the prevention and treatment of ageing and age-related diseases. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00280836
Volume :
510
Issue :
7505
Database :
Academic Search Index
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
96771801
Full Text :
https://doi.org/10.1038/nature13264